1. FDA should further integrate its review of cybersecurity into the premarket review process for medical devices Publication: [Washington, D.C.] : U.S. Department of Health and Human Services, Office of Inspector General, September 2018 Subject(s): Computer SecurityDevice Approval -- standardsEquipment and Supplies -- standardsEquipment Safety -- standardsComputer Communication Networks -- standardsGuidelines as TopicSoftware -- standardsHumansUnited StatesUnited States. Department of Health and Human Services.United States. Food and Drug Administration.
2. Deciding when to submit a 510(k) for a software change to an existing device: guidance for industry and Food and Drug Administration staff Publication: Silver Spring, MD : Center for Devices and Radiological Health, October 25, 2017 Subject(s): Device Approval -- standardsSoftware -- standardsComputer SecurityEquipment Design -- standardsEquipment Safety -- standardsHumansUnited StatesUnited States. Department of Health and Human Services.United States. Food and Drug Administration.
